To report SUSPECTED ADVERSE REACTIONS, contact argenx at 1-833-argx411 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch
Resource Library
To report SUSPECTED ADVERSE REACTIONS, contact argenx at 1-833-argx411 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch
To report SUSPECTED ADVERSE REACTIONS, contact argenx at 1-833-argx411 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch
Diagnosis and Referral Resources
Resources to inform recognition and diagnosis of CMS
Resources designed to inform recognition and diagnosis of CMS
This resource hub brings together key information including diagnostic features, genetic confirmation, specialist referral, and clinical trial opportunities.
If it could be CMS, order a free genetic test to diagnose, or refer to a specialist for support
Diagnosing CMS
Review this resource to explore CMS diagnosis, including clinical signs that raise suspicion, key differential considerations, and the role of genetic testing in confirming the diagnosis
How to access free genetic testing for people with suspected CMS
Review this resource for practical guidance on accessing free genetic testing, a service offered by Invitae, including eligibility criteria, how to initiate testing, gene coverage, complimentary genetic counseling for individuals with a positive result, and support for integrating testing into clinical practice
How to refer people with suspected CMS to a specialist
Review this resource to identify CMS specialists accepting referrals, particularly for complex or unclear cases, and for practical guidance on when to refer, key eligibility criteria, referral processes, and key contact details
If it is CMS, consider referring your patient for enrollment into a clinical study to improve understanding of the disease
CMS clinical studies led by argenx
Natural history study
Investigating DOK7-, MuSK-, AGRN-, and LRP4-CMS (NCT06078553)
Additional CMS information
Overview
Explore an overview of CMS, their key clinical features, and common misdiagnoses
Educational events
Find information on live and virtual events designed to enhance your understanding of CMS and their diagnosis
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